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VAS-CATH DUALATOR(TM) VESSEL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914210
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/1/1993
Days to Decision
651 days
Submission Type
Statement

VAS-CATH DUALATOR(TM) VESSEL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914210
510(k) Type
Traditional
Applicant
VAS-CATH, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/1/1993
Days to Decision
651 days
Submission Type
Statement